Hi, folks. Hope it's a wonderful, pain-free day for you all.
Listen, my GP suspects I have Lupus. I have several of the symptoms and we will get to the blood work as soon as he becomes effective on my insurance. Long story there.
Anyway, I don't want to be lead to websites to find out about this auto-immune disease, I would much rather know about "your" personal experiences or that of someone you know who has had lupus.
I know that symptoms can differ from case to case, so I was interested in hearing how it's affected others and their quality of living. Can this be managed, supressed...?
Thanks so much for all of your help. It's greatly appreciated.